Canonical Allele Identifier: CA1619117536

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354647T= , CM000668.2:g.31354647T=	GRCh38
NC_000006.11:g.31322424T= , CM000668.1:g.31322424T=	GRCh37
NC_000006.10:g.31430403T=	NCBI36
NG_023187.1:g.7566A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3078A=
ENST00000481849.6:n.3038A=
ENST00000497377.6:n.2945A=
ENST00000640094.2:c.914A=	ENSP00000491275.2:p.Tyr305=
ENST00000696558.1:c.1100A=	ENSP00000512716.1:n.1100A=
ENST00000696559.1:c.1031A=	ENSP00000512717.1:p.Tyr344=
ENST00000696560.1:c.1031A=	ENSP00000512718.1:p.Tyr344=
ENST00000696561.1:c.1031A=	ENSP00000512719.1:p.Tyr344=
ENST00000696562.1:c.1031A=	ENSP00000512720.1:p.Tyr344=
ENST00000412585.7:c.1031A= MANE Select	ENSP00000399168.2:p.Tyr344=
ENST00000640094.1:c.107A=	ENSP00000491275.1:p.Tyr36=
ENST00000412585.6:c.1031A=	ENSP00000399168.2:p.Tyr344=
ENST00000481849.5:n.160A=
ENST00000497377.5:n.430A=
NM_005514.6:c.1031A=	NP_005505.2:p.Tyr344=
XM_011514556.1:c.1064A=	XP_011512858.1:p.Tyr355=
XM_011514557.1:c.914A=	XP_011512859.1:p.Tyr305=
XR_926175.1:n.1470A=
NM_005514.7:c.1031A=	NP_005505.2:p.Tyr344=
NM_005514.8:c.1031A= MANE Select	NP_005505.2:p.Tyr344=